Stanley F. Nelson
Molecular Biology · 2006–2015
A researcher in the Science corpus: 17 papers; trusts 6 researchers and is trusted by 6 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 122 citations into it; #12,028 of 17,773 by trust here, #2,878 by citations
- Genetics — 117 citations into it; #3,733 of 6,854 by trust here, #231 by citations
- Computational Biology & Bioinformatics — 7 citations into it
Whom Stanley F. Nelson trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Stanley F. Nelson overall
Papers from Stanley F. Nelson's perspective
Ordered by how strongly the researchers Stanley F. Nelson trusts endorse each paper. Same corpus, a different order for every researcher.
- Identification of common molecular subsequences.
- BLAT--the BLAST-like alignment tool. (Genome Research)
- SSAHA: a fast search method for large DNA databases. (Genome Research)
- SOAP: short oligonucleotide alignment program (Bioinform.)
- Mapping short DNA sequencing reads and calling variants using mapping quality scores. (Genome Research)
- Ultrafast and memory-efficient alignment of short DNA sequences to the human genome (Genome Biology)
- Lethality and centrality in protein networks
- Hierarchical Organization of Modularity in Metabolic Networks (Science)
- Genome sequencing in microfabricated high-density picolitre reactors (Nature)
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.
Their papers
- BFAST: An Alignment Tool for Large Scale Genome Resequencing (2009) — 586 citations
- Assessing the significance of chromosomal aberrations in cancer: Methodology and application to glioma (2007) — 1,099 citations
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (2010) — 2,055 citations
- Melanomas acquire resistance to B-RAF(V600E) inhibition by RTK or N-RAS upregulation (2010) — 2,217 citations
- Melanoma whole exome sequencing identifies V600EB-RAF amplification-mediated acquired B-RAF inhibitor resistance (2012) — 643 citations
- Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) — 750 citations
- Clinical Exome Sequencing for Genetic Identification of Rare Mendelian Disorders (2014) — 985 citations
- Targeted Therapy Resistance Mediated by Dynamic Regulation of Extrachromosomal Mutant EGFR DNA (2013) — 628 citations
- DNA sequencing of maternal plasma to detect Down syndrome: An international clinical validation study (2011) — 903 citations
- Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV (2011) — 407 citations
- A genome-wide scan for common alleles affecting risk for autism (2010) — 601 citations
- Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterning (2008) — 2,259 citations
- Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays (2008) — 1,347 citations
- Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia (2008) — 1,770 citations
- Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. (2008) — 844 citations
- High-throughput oncogene mutation profiling in human cancer (2007) — 1,054 citations
- Gene connectivity, function, and sequence conservation: predictions from modular yeast co-expression networks (2006) — 363 citations